Incidental Appendiceal Neuroendocrine Tumors (NETs): A Case Report and Review Of Literature
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Creator 1. Peerawitch Petchmak
2. Punnawat Chandrachamnong
Title Incidental Appendiceal Neuroendocrine Tumors (NETs): A Case Report and Review Of Literature
Publisher Text and Journal Publication
Publication Year 2565
Journal Title Vajira Medical Journal
Journal Vol. 66
Journal No. 3
Page no. 229-236
Keyword appendix, appendicitis, appendiceal neuroendocrine tumors, carcinoid tumors, NET G2
URL Website https://tci-thaijo.org/index.php/VMED
Website title Vajira Medical Journal (วชิรเวชสาร)
ISSN 0125-1252
Abstract Incidental appendiceal neuroendocrine tumors (NETs) are rare and mostly asymptomatic or come with clinically suspected appendicitis. Although, there is a various review of literatures and consensus guidelines, there has been controversy in the management of tumor size 1-2 cm or grading G2 G3 according to mitotic count (mitoses/10 HPF) or Ki-67. A 20-year-old female presented to the emergency department with acute right lower quadrant abdominal pain with an onset of 2 hours. The presumed clinical diagnosis was acute appendicitis. She underwent an open appendectomy and the histopathologic result of the specimen showed a neuroendocrine tumor of the appendix. It was a controversial decision since it was a well-differentiated tumor of <1 cm as well as G2 at the distal half of the appendix, which made it a challenging surgery. The patient was informed and computer tomography (CT) scan and colonoscopy was done for further evaluation. Discussion of whether a right-hemicolectomy or single appendectomy was proposed to the patient, finally a right hemicolectomy was performed. However, more studies should be conducted to determine the optimal management and follow-up strategy for situations like this.
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